Removal of Carbaryl Pesticide from Aqueous Solution by Adsorption on Local Clay in Agadir

This study was conducted to assess the removal efficiency of pesticide (Carbaryl) used in Souss Massa region (Agadir city), on a clay originated from barrage situated in Agadir. The adsorption of Carbaryl from aqueous solution by local clay as a low-cost, natural and eco-friendly adsorbent was investigated. Different physicochemical parameters were analyzed: adsorbent mass, ionic strength (NaNO3), initial concentration of pollutant, temperature, and pH. The empirical results showed that all these parameters have an impact on the retention of pesticide on the clay. The equilibrium uptake was increased with an increase in the initial pesticide concentration in solution. The results of adsorption were fitted to the Langmuir and Freundlich isotherms. The Freundlich model represented the adsorption process better than Langmuir model, with correlation coefficients (R2) values ranged from 0.97 to 0.99. This study has shown that the natural clay is a solid that has got an important adsorption capacity, which may be used in treatment and depollution of water.

Removal from Water and Adsorption onto Natural Quartz Sand of Hydroquinone

Hydroquinone (HQ) is the most important hydroxy aromatic compound which is produced on a large scale. Understanding its fate in the environment is therefore of primary importance to prevent its migration in the soil and/or the contamination of the aquatic ecosystems. Here we present a column based method to investigate the physicochemical processes controlling the removal from the aqueous phase and the adsorption onto natural quartz sand (NQS), of organic pollutant such as HQ molecules. We will focus on the interactions that occur between the organic pollutant and the NQS substrate. Thus, column reactors filled with NQS were used to investigate the influence of physicochemical parameters such as the ionic strength, the pH, the flow rate, and the nature of the electrolyte cation, on the HQ adsorption from water onto NQS substrate. The data indicate that, when divalent instead of monovalent cations, are present in the effluent water injection phase, and/or when the ionic strength of the effluent increases, the adsorbed HQ amount decreases. Similar decrease of the adsorbed HQ amount was also observed, at constant ionic strength, by increasing either, the pH from 3 to 9, the flow rate Q from 1 to 3 ml·mn-1, or by decreasing the HQ initial concentration, C0 from 30 to 6 mg·L-1. Further, large amount of the organic pollutant (up to 93 wt% of HQ molecules) was removed from the effluent water phase by using NQS column. The overall data seem to indicate that the adsorption of HQ molecules on the NQS surface is mainly controlled by electrostatic interaction forces occurring between the organic molecule polar groups and the inorganic matrix silanol groups.

Effective Removal of Nitrates Ions from Aqueous Solution Using New Clay as Potential Low-Cost Adsorbent

In the present study, we investigated the performance of clay mineral originated from a dam situated in Morocco (Agadir city), as natural, low-cost, alternative and eco-friendly adsorbent for removal of nitrates ions from aqueous solution within a batch process. The clay was characterized by X-ray diffraction, Scanning Electron Microscopy (SEM), Dispersive Energy of Spectroscopy (EDS), Fourier Transform Infrared (FTIR) and surface area analysis (BET). The effects of various experimental parameters are examined such as contact time, initial concentration of pollutant, adsorbent mass and solution pH. The removal of nitrate was 71.89% at natural pH (pH = 5.1) using 1 g/l of adsorbent in 500 ml of nitrate solution having initial concentration of 300 mg/l (effect of contact time). Adsorption kinetic study revealed that the adsorption process followed first order kinetic. Theoretical correlation of the experimental equilibrium adsorption data for the Nitrate-New Clay system was properly explained by the Langmuir isotherm model. The maximum adsorption capacity was Qm, exp = 244.06 mg/g at 20℃ and at natural pH (with Qm, cal = 250 mg/g). An increase in adsorbent dosage increased the percent removal of nitrate, R = 1 g/l was considered as optimum dose and was used for further study. The pH heavily affected the adsorption capacity, and the percentage removal was found to decrease with increase in pH. The obtained results indicated that this New Clay (NC) was very good adsorbent for NO3-, interesting alternative material with respect to more costly adsorbent used, and could be used as a highly efficient adsorbent for the separation of nitrate from drinking or waste water.